Clin2
NCT07502664Possibly a fitRecruiting

A study on vision and navigation in inherited retinal disease

Retinitis PigmentosaStargardt Macular DystrophyStargardt DiseaseGeographic Atrophy From Age-related Macular DegenerationX-linked RetinoschisisRetinal Dystrophies

Part of Eyes & vision, Genetic & congenital clinical trials.

This study is looking at how people with inherited retinal disease that affects peripheral vision see and move around. It will test a new way to measure vision and navigation to see if it can help doctors understand how the disease affects daily life.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
25 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You have been diagnosed with retinitis pigmentosa or another inherited retinal disease that affects your side vision.
  • Your best corrected vision in at least one eye is between 20/200 and hand motion.
  • You are reasonably fluent in English or Spanish.
  • You do not have severe memory loss or dementia that would make it hard to follow the study.
  • You are not pregnant.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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